Variant report

Variant	nsv1059134
Chromosome Location	chr21:29061408-29188185
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:905)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:905 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr21:29110010-29110027	K562	blood:	n/a	n/a
2	ATF2	chr21:29073392-29073757	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr21:29073346-29073703	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr21:29073430-29073632	HepG2	liver:	n/a	n/a
5	BRCA1	chr21:29073324-29073714	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr21:29077225-29077425	IMR90	lung:	n/a	chr21:29077309-29077320
7	CEBPB	chr21:29072742-29073030	IMR90	lung:	n/a	n/a
8	CEBPB	chr21:29073256-29073935	Hela-S3	cervix:	n/a	chr21:29073413-29073424
9	CEBPB	chr21:29136486-29136690	A549	lung:	n/a	chr21:29136550-29136561
10	CEBPB	chr21:29140574-29140759	IMR90	lung:	n/a	n/a
11	CEBPB	chr21:29077177-29077377	HepG2	liver:	n/a	chr21:29077309-29077320
12	CEBPB	chr21:29106521-29107013	IMR90	lung:	n/a	chr21:29106848-29106861
13	CEBPB	chr21:29159283-29159763	HepG2	liver:	n/a	chr21:29159609-29159620
14	CEBPB	chr21:29065710-29066038	IMR90	lung:	n/a	n/a
15	CEBPB	chr21:29084470-29084512	IMR90	lung:	n/a	n/a
16	CEBPB	chr21:29073307-29073727	H1-hESC	embryonic stem cell:	n/a	chr21:29073413-29073424
17	CEBPB	chr21:29136389-29136701	IMR90	lung:	n/a	chr21:29136550-29136561
18	CEBPB	chr21:29178101-29178422	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr21:29085985-29086187	IMR90	lung:	n/a	n/a
20	CEBPB	chr21:29073252-29073904	IMR90	lung:	n/a	chr21:29073413-29073424
21	CEBPB	chr21:29159437-29159735	IMR90	lung:	n/a	chr21:29159609-29159620
22	CEBPB	chr21:29116343-29116435	HepG2	liver:	n/a	n/a
23	CEBPB	chr21:29159522-29159680	A549	lung:	n/a	chr21:29159609-29159620
24	CEBPB	chr21:29136390-29136692	HepG2	liver:	n/a	chr21:29136550-29136561
25	CEBPB	chr21:29073319-29073793	HepG2	liver:	n/a	chr21:29073413-29073424
26	CEBPB	chr21:29184627-29184943	IMR90	lung:	n/a	n/a
27	CHD1	chr21:29073123-29073951	IMR90	lung:	n/a	n/a
28	CTCF	chr21:29175320-29175470	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr21:29131340-29131490	GM12866	blood:	n/a	n/a
30	CTCF	chr21:29131436-29131896	Fibrobl	skin:	n/a	n/a
31	CTCF	chr21:29073460-29073610	AG04449	skin:	n/a	chr21:29073500-29073510 chr21:29073497-29073515 chr21:29073492-29073513 chr21:29073499-29073512
32	CTCF	chr21:29131480-29131630	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr21:29061540-29061690	AG04449	skin:	n/a	n/a
34	CTCF	chr21:29073460-29073610	GM12874	blood:	n/a	chr21:29073500-29073510 chr21:29073497-29073515 chr21:29073492-29073513 chr21:29073499-29073512
35	CTCF	chr21:29175280-29175430	HEK293	kidney:	n/a	n/a
36	CTCF	chr21:29175340-29175490	GM12866	blood:	n/a	n/a
37	CTCF	chr21:29132240-29132390	AG09319	gingival:	n/a	n/a
38	CTCF	chr21:29131520-29131670	NB4	blood:	n/a	n/a
39	CTCF	chr21:29132200-29132350	HPF	lung:	n/a	n/a
40	CTCF	chr21:29131520-29131670	NHLF	lung:	n/a	n/a
41	CTCF	chr21:29132240-29132390	HFF	foreskin:	n/a	n/a
42	CTCF	chr21:29175260-29175410	GM12864	blood:	n/a	n/a
43	CTCF	chr21:29073411-29073636	GM13976	blood:	n/a	chr21:29073500-29073510 chr21:29073497-29073515 chr21:29073492-29073513 chr21:29073499-29073512
44	CTCF	chr21:29073406-29073657	MCF-7	breast:	n/a	chr21:29073500-29073510 chr21:29073497-29073515 chr21:29073492-29073513 chr21:29073499-29073512
45	CTCF	chr21:29175280-29175430	GM12865	blood:	n/a	n/a
46	CTCF	chr21:29131520-29131670	AG09309	skin:	n/a	n/a
47	CTCF	chr21:29175319-29175485	GM13977	blood:	n/a	n/a
48	CTCF	chr21:29131520-29131670	GM12873	blood:	n/a	n/a
49	CTCF	chr21:29073360-29073510	HCT-116	colon:	n/a	chr21:29073500-29073510
50	CTCF	chr21:29131391-29131786	H1-hESC	embryonic stem cell:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:29099379-29099429	GM12892	blood:	n/a
2	chr21:29099379-29099429	GM12891	blood:	n/a
3	chr21:29099379-29099429	Hela-S3	cervix:	n/a
4	chr21:29093202-29093252	HCPEpiC	choroid plexus:	n/a
5	chr21:29099379-29099429	NH-A	brain:	n/a
6	chr21:29093202-29093252	ProgFib	skin:	n/a
7	chr21:29099379-29099429	HUVEC	blood vessel:	n/a
8	chr21:29099379-29099429	SAEC	small airway:	n/a
9	chr21:29099379-29099429	HEK293	kidney:	embryo
10	chr21:29099379-29099429	HCM	heart:	n/a
11	chr21:29093202-29093252	A549	lung:	n/a
12	chr21:29093202-29093252	SK-N-SH_RA	brain:	n/a
13	chr21:29093202-29093252	NHDF-neo	bronchial:	n/a
14	chr21:29093202-29093252	GM12878	blood:	n/a
15	chr21:29099379-29099429	PANC-1	pancreas:	n/a
16	chr21:29099379-29099429	H1-hESC	embryonic stem cell:	embryo
17	chr21:29093202-29093252	RPTEC	kidney:	n/a
18	chr21:29099379-29099429	AG04450	lung:	fetal
19	chr21:29093202-29093252	HL-60	blood:	n/a
20	chr21:29099379-29099429	T-47D	breast:	n/a
21	chr21:29093202-29093252	AG09309	skin:	n/a
22	chr21:29093202-29093252	SAEC	small airway:	n/a
23	chr21:29099379-29099429	HCF	heart:	n/a
24	chr21:29099379-29099429	Jurkat	blood:	n/a
25	chr21:29099379-29099429	HRCEpiC	kidney:	n/a
26	chr21:29093202-29093252	HEEpiC	esophagus:	n/a
27	chr21:29099379-29099429	AoSMC	blood vessel:	n/a
28	chr21:29093202-29093252	Caco-2	colon:	n/a
29	chr21:29099379-29099429	ECC-1	luminal epithelium:	n/a
30	chr21:29099379-29099429	Caco-2	colon:	n/a
31	chr21:29099379-29099429	MCF-7	breast:	n/a
32	chr21:29099379-29099429	K562	blood:	n/a
33	chr21:29093202-29093252	HIPEpiC	eye:	n/a
34	chr21:29093202-29093252	GM12892	blood:	n/a
35	chr21:29093202-29093252	NT2-D1	testis:	n/a
36	chr21:29093202-29093252	HRE	kidney:	n/a
37	chr21:29093202-29093252	GM12891	blood:	n/a
38	chr21:29099379-29099429	HepG2	liver:	n/a
39	chr21:29099379-29099429	NB4	blood:	n/a
40	chr21:29093202-29093252	PFSK-1	brain:	n/a
41	chr21:29093202-29093252	T-47D	breast:	n/a
42	chr21:29099379-29099429	SK-N-SH_RA	brain:	n/a
43	chr21:29093202-29093252	GM19239	blood:	n/a
44	chr21:29099379-29099429	SKMC	muscle:	n/a
45	chr21:29099379-29099429	AG09319	gingival:	n/a
46	chr21:29093202-29093252	AG10803	skin:	n/a
47	chr21:29093202-29093252	CMK	blood:	n/a
48	chr21:29093202-29093252	HMEC	breast:	n/a
49	chr21:29099379-29099429	SK-N-MC	brain:	n/a
50	chr21:29093202-29093252	H1-hESC	embryonic stem cell:	embryo

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:28222055..28222830-chr21:29073096..29074079,2	K562	blood:
2	chr21:29130365..29132734-chr21:29133407..29135689,2	K562	blood:
3	chr21:28221528..28223154-chr21:29072525..29074611,26	MCF-7	breast:
4	chr21:28221411..28222029-chr21:29073057..29074050,3	K562	blood:
5	chr21:28222266..28223005-chr21:29072932..29073598,4	MCF-7	breast:
6	chr21:29130365..29132734-chr21:29133407..29135689,2	K562	blood:
7	chr21:28104973..28105545-chr21:29073049..29073643,2	MCF-7	breast:
8	chr21:29131169..29131808-chr21:29708353..29709051,2	MCF-7	breast:
9	chr21:28221585..28222726-chr21:29073735..29074729,3	MCF-7	breast:
10	chr1:113346446..113346980-chr21:29107601..29108558,2	MCF-7	breast:
11	chr21:28141720..28142490-chr21:29073373..29073879,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP16-6	chr21:29123391-29123557	NONHSAT081584
2	lnc-USP16-6	chr21:29118675-29118913	FPKM1_group_20009_transcript_1
3	lnc-USP16-6	chr21:29097118-29097200	ENSG00000225298
4	lnc-USP16-6	chr21:29115712-29115823	ENSG00000225298
5	lnc-USP16-6	chr21:29123391-29123524	FPKM1_group_20009_transcript_1
6	lnc-USP16-6	chr21:29118617-29118913	NONHSAT081584
7	lnc-USP16-6	chr21:29118137-29118355	ENSG00000225298
8	lnc-USP16-6	chr21:29118137-29118351	ENSG00000225298
9	lnc-USP16-6	chr21:29094717-29094732	ENSG00000225298
10	lnc-USP16-6	chr21:29123391-29123552	ENSG00000225298
11	lnc-USP16-6	chr21:29094698-29094732	XLOC_013897
12	lnc-USP16-6	chr21:29115712-29115823	ENSG00000225298
13	lnc-USP16-6	chr21:29123391-29123552	XLOC_013897
14	lnc-USP16-6	chr21:29115712-29115823	XLOC_013897
15	lnc-USP16-6	chr21:29118137-29118351	XLOC_013897
16	lnc-USP16-6	chr21:29123391-29123552	ENSG00000225298

No data

Variant related genes	Relation type
LINC00113	TF binding region
LINC00113	CpG island

Extended variants
information (count: 4139 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4139 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115561107	chr21:29061430-29061431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114431628	chr21:29061438-29061439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73386062	chr21:29061439-29061440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537573499	chr21:29061470-29061471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1431367	chr21:29061478-29061479	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs527278570	chr21:29061495-29061496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571459730	chr21:29061498-29061499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs80271593	chr21:29061536-29061537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs9982537	chr21:29061554-29061555	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs9983211	chr21:29061560-29061561	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs573210873	chr21:29061587-29061588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545152743	chr21:29061589-29061590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9982546	chr21:29061605-29061606	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs574962790	chr21:29061608-29061609	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544330599	chr21:29061642-29061643	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560697285	chr21:29061676-29061677	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141031584	chr21:29061690-29061691	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144739064	chr21:29061769-29061770	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560445797	chr21:29061770-29061771	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78432306	chr21:29061775-29061776	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547249294	chr21:29061793-29061794	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552370721	chr21:29061804-29061805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377108840	chr21:29061816-29061817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569088384	chr21:29061838-29061839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375482097	chr21:29061845-29061846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527449109	chr21:29061857-29061858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551101675	chr21:29061877-29061878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567543928	chr21:29061906-29061907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536610036	chr21:29061925-29061926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552953608	chr21:29061931-29061932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2831085	chr21:29061934-29061935	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs9653692	chr21:29061947-29061948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs558713540	chr21:29061971-29061972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73183756	chr21:29061981-29061982	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs546202093	chr21:29061996-29061997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187783947	chr21:29062022-29062023	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574455468	chr21:29062028-29062029	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138657576	chr21:29062060-29062061	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560211587	chr21:29062072-29062073	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532413816	chr21:29062127-29062128	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9653693	chr21:29062132-29062133	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs243656	chr21:29062139-29062140	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs13046254	chr21:29062149-29062150	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs548094248	chr21:29062152-29062153	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567706492	chr21:29062204-29062205	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530160363	chr21:29062207-29062208	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146990682	chr21:29062214-29062215	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547680113	chr21:29062219-29062220	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190921888	chr21:29062271-29062272	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75596697	chr21:29062356-29062357	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	21251322	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	22174824	CNVD
Renal cell carcinoma	18765545	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	18160780	CNVD
Mental retardation	17621639	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	20164919	CNVD

Chromatin state (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:29054600-29061600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr21:29061600-29061800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr21:29061800-29062000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr21:29062000-29062600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr21:29062600-29064800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr21:29063000-29063200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr21:29063000-29063200	Enhancers	Colon Smooth Muscle	Colon
8	chr21:29063000-29063400	Enhancers	Rectal Smooth Muscle	rectum
9	chr21:29063000-29063800	Enhancers	Fetal Lung	lung
10	chr21:29063200-29063800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr21:29063400-29065400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr21:29063600-29063800	Enhancers	HSMM	muscle
13	chr21:29063600-29064000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr21:29063800-29064000	Enhancers	Osteobl	bone
15	chr21:29063800-29064800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr21:29063800-29065400	Weak transcription	HSMM	muscle
17	chr21:29064000-29065000	Weak transcription	Osteobl	bone
18	chr21:29064000-29066400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr21:29064800-29065400	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr21:29064800-29065600	Enhancers	HMEC	breast
21	chr21:29064800-29067400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr21:29065000-29065800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr21:29065000-29065800	Enhancers	Osteobl	bone
24	chr21:29065200-29065400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr21:29065200-29065600	Enhancers	NHEK	skin
26	chr21:29065200-29065800	Enhancers	HSMMtube	muscle
27	chr21:29065200-29066200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr21:29065400-29065800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr21:29065400-29065800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
30	chr21:29065400-29065800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr21:29065400-29065800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr21:29065400-29066200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr21:29065400-29066200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr21:29065400-29066200	Enhancers	Muscle Satellite Cultured Cells	--
35	chr21:29065400-29066200	Enhancers	HSMM	muscle
36	chr21:29065400-29066200	Enhancers	NHDF-Ad	bronchial
37	chr21:29065600-29065800	Flanking Active TSS	HMEC	breast
38	chr21:29065600-29065800	Flanking Active TSS	NHEK	skin
39	chr21:29065600-29066200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr21:29065600-29066200	Enhancers	NHLF	lung
41	chr21:29065800-29066000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr21:29065800-29066000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr21:29065800-29066000	Enhancers	HMEC	breast
44	chr21:29065800-29066000	Enhancers	NHEK	skin
45	chr21:29065800-29066200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr21:29065800-29066200	Flanking Active TSS	Osteobl	bone
47	chr21:29065800-29067000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr21:29065800-29073600	Weak transcription	HSMMtube	muscle
49	chr21:29066000-29066200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr21:29066000-29066200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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